CN117199576A - Charging method of lithium battery with silicon-containing negative electrode - Google Patents
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Abstract
本发明提供一种含硅负极的锂电池的充电方法,其特征在于:包括第一充电阶段和第二充电阶段;在第一充电阶段中,采用C1倍率充电;在第二充电阶段中,采用C2倍率充电;其中,C1和C2满足以下关系式:C1=n1×n2×C2×(P1×W1)/(P1×W1+P2×W2);其中,n1=0.3~0.7,n2=3.6‑5×W1;C2=1.25~12;其中,在含硅负极中,负极活性物质包括硅和石墨,P1表示硅可逆容量,P2表示石墨可逆容量,W1表示硅含量,W2表示石墨含量;在锂电池的充电过程中,当第一充电阶段中锂电池的SOC值到达阈值a,第一充电阶段结束,切换为第二充电阶段;其中,a=n1×(P1×W1)/(P1×W1+P2×W2)。本发明的充电方法有利于提高硅颗粒在充电过程的稳定性,保证硅颗粒容量的长期发挥、优化电池循环性能以及减少充电时间。The invention provides a charging method for a lithium battery containing a silicon negative electrode, which is characterized in that it includes a first charging stage and a second charging stage; in the first charging stage, C1 rate charging is used; in the second charging stage, using C2 rate charging; among them, C1 and C2 satisfy the following relationship: C1=n1×n2×C2×(P1×W1)/(P1×W1+P2×W2); among them, n1=0.3~0.7, n2=3.6‑ 5×W1; C2=1.25~12; among them, in the silicon-containing negative electrode, the negative active material includes silicon and graphite, P1 represents the reversible capacity of silicon, P2 represents the reversible capacity of graphite, W1 represents the silicon content, and W2 represents the graphite content; in lithium During the charging process of the battery, when the SOC value of the lithium battery reaches the threshold a in the first charging stage, the first charging stage ends and switches to the second charging stage; where, a=n1×(P1×W1)/(P1×W1 +P2×W2). The charging method of the present invention is beneficial to improving the stability of silicon particles during the charging process, ensuring the long-term capacity of the silicon particles, optimizing battery cycle performance and reducing charging time.
Description
技术领域Technical field
本发明属于锂电池技术领域,具体涉及一种含硅负极的锂电池的充电方法。The invention belongs to the technical field of lithium batteries, and specifically relates to a charging method of a lithium battery containing a silicon negative electrode.
背景技术Background technique
析锂是影响锂离子电池快充的主要原因,析锂是指锂离子直接在负极表面还原为金属锂而不是进入负极中。在锂离子电池快速充电过程中,电池内部存在巨大的极化,包括欧姆阻抗、浓差过电势和电荷转移过电势,这会导致很大的电压损失。Lithium precipitation is the main reason that affects the fast charging of lithium-ion batteries. Lithium precipitation means that lithium ions are directly reduced to metallic lithium on the surface of the negative electrode instead of entering the negative electrode. During the fast charging process of lithium-ion batteries, there is huge polarization inside the battery, including ohmic impedance, concentration overpotential and charge transfer overpotential, which will lead to large voltage loss.
在目前所发现的锂离子电池负极材料中,硅基材料的理论质量比容量最高,为4200mAh·g-1,另外,硅基材料对母体的嵌入电位比石墨类材料略高,不易在材料表面形成枝晶而引发安全性问题,这些都使得硅基材料成为极具潜力和吸引力的负极材料。Among the lithium-ion battery anode materials discovered so far, silicon-based materials have the highest theoretical mass specific capacity, which is 4200mAh·g -1 . In addition, the embedding potential of silicon-based materials into the matrix is slightly higher than that of graphite materials, and it is not easy to embed on the surface of the material. The formation of dendrites raises safety issues, which make silicon-based materials a very potential and attractive anode material.
而在目前的硅基负极材料中,硅/石墨负极材料因硅、石墨原料易获取,且这两种材料具有相对稳定的电化学性能而被广泛研究与应用。而硅作为一种半导体材料,其本身离子迁移能力差,按照现有的阶梯充电策略,每一步快充常根据快充时间要求计算最高倍率然后依次降阶,这种方法在快充开始时就对电池施加较大的充电倍率,这样会使得脱嵌锂动力学较差的硅颗粒承受很高的内部应力,容易导致硅颗粒破碎,不利于硅基负极材料长期性能的发挥,加速快充循环过程中的容量衰减。且在这种方法中,因为硅颗粒一开始无法适应快速的脱嵌锂速率,导致电池极化现象加剧,输入电压无法与充电量相对应,即造成输入能量的无效损失,最终也会导致充电时间的延长,Among the current silicon-based anode materials, silicon/graphite anode materials are widely researched and used because silicon and graphite raw materials are easy to obtain, and these two materials have relatively stable electrochemical properties. As a semiconductor material, silicon has poor ion migration ability. According to the existing ladder charging strategy, each step of fast charging usually calculates the highest rate according to the fast charging time requirements and then reduces the steps in sequence. This method starts at the beginning of fast charging. Applying a large charging rate to the battery will cause the silicon particles with poor lithium deintercalation kinetics to bear high internal stress, which will easily cause the silicon particles to break, which is not conducive to the long-term performance of the silicon-based anode material and accelerates fast charging cycles. Capacity fading during the process. And in this method, because the silicon particles cannot adapt to the rapid deintercalation rate of lithium at the beginning, the polarization phenomenon of the battery is intensified, and the input voltage cannot correspond to the charging amount, which results in ineffective loss of input energy and ultimately leads to charging the extension of time,
有鉴于此,提供一种适合硅/石墨负极的锂电池的充电方法,提高电池循环容量性能和充电效率,具有重大的实际意义。In view of this, it is of great practical significance to provide a charging method for lithium batteries suitable for silicon/graphite negative electrodes to improve battery cycle capacity performance and charging efficiency.
发明内容Contents of the invention
为解决现有技术中存在的问题与不足,本发明提供一种含硅负极的锂电池的充电方法,该充电方法有利于提高硅颗粒在充电过程的稳定性,保证硅颗粒容量的长期发挥、优化电池循环性能以及减少充电时间。In order to solve the problems and deficiencies existing in the prior art, the present invention provides a charging method for lithium batteries containing silicon negative electrodes. This charging method is beneficial to improving the stability of silicon particles during the charging process and ensuring the long-term performance of the silicon particle capacity. Optimize battery cycle performance and reduce charging time.
本发明提供一种含硅负极的锂电池的充电方法,包括第一充电阶段和第二充电阶段;在第一充电阶段中,采用C1倍率充电;在第二充电阶段中,采用C2倍率充电;其中,C1和C2满足以下关系式:C1=n1×n2×C2×(P1×W1)/(P1×W1+P2×W2);其中,n1=0.3~0.7,n2=3.6-5×W1;C2=1.25~12;其中,在含硅负极中,负极活性物质包括硅和石墨,P1表示硅可逆容量,P2表示石墨可逆容量,W1表示硅含量,W2表示石墨含量;在锂电池的充电过程中,当第一充电阶段中锂电池的SOC值到达阈值a,第一充电阶段结束,切换为第二充电阶段;其中,a=n1×(P1×W1)/(P1×W1+P2×W2)。The invention provides a charging method for a lithium battery containing a silicon negative electrode, which includes a first charging stage and a second charging stage; in the first charging stage, C1 rate charging is used; in the second charging stage, C2 rate charging is used; Among them, C1 and C2 satisfy the following relationship: C1=n1×n2×C2×(P1×W1)/(P1×W1+P2×W2); among them, n1=0.3~0.7, n2=3.6-5×W1; C2=1.25~12; among them, in the silicon-containing negative electrode, the negative active material includes silicon and graphite, P1 represents the silicon reversible capacity, P2 represents the graphite reversible capacity, W1 represents the silicon content, and W2 represents the graphite content; during the charging process of lithium battery , when the SOC value of the lithium battery reaches the threshold a in the first charging stage, the first charging stage ends and switches to the second charging stage; where, a=n1×(P1×W1)/(P1×W1+P2×W2 ).
在上述公式中,硅可逆含量(P1)表示硅负极片(这里硅负极片指负极活性物质只有硅)制成的半电池首次脱锂克容量;半电池制作过程如下:取1.5g碳纳米管(CNT)及15g固含量为1.4%的羧甲基纤维素(CMC)胶液匀浆,再称取0.09g导电炭黑(SP),称取2.7g负极活性物质,加水9g搅拌均匀后,将得到的负极浆料在负极集流体上涂布350μm,80℃烘2小时,得到负极片;将上述负极片与锂箔片组成扣式电池,搁置至少12小时;测试方法如下:静置2h;0.1C倍率放电至5mv;0.05C倍率放电至5mv;0.02C倍率放电至5mv;0.01C倍率放电至5mv;0.1C倍率充电至2V;随后计算硅可逆容量。在这里,硅可逆容量=硅(脱锂容量/负极活性物质质量;倍率公式里的可逆容量已经归一化为克容量。In the above formula, the silicon reversible content (P1) represents the first delithiation capacity of a half-battery made of a silicon negative electrode sheet (here the silicon negative electrode sheet means that the negative active material is only silicon); the half-cell production process is as follows: take 1.5g of carbon nanotubes (CNT) and 15g of carboxymethylcellulose (CMC) glue solution with a solid content of 1.4%, then weigh 0.09g of conductive carbon black (SP), weigh 2.7g of negative active material, add 9g of water and stir evenly. Coat the obtained negative electrode slurry with a thickness of 350 μm on the negative electrode current collector and bake it at 80°C for 2 hours to obtain a negative electrode sheet; combine the above negative electrode sheet and lithium foil to form a button battery and leave it aside for at least 12 hours; the test method is as follows: let it stand for 2 hours ; 0.1C rate discharge to 5mv; 0.05C rate discharge to 5mv; 0.02C rate discharge to 5mv; 0.01C rate discharge to 5mv; 0.1C rate charge to 2V; then calculate the silicon reversible capacity. Here, silicon reversible capacity = silicon (delithiation capacity/mass of negative active material; the reversible capacity in the rate formula has been normalized to gram capacity.
石墨可逆容量(P2)表示石墨可逆容量指石墨负极片(这里石墨负极片指负极活性物质只有石墨)制成的半电池首次脱锂克容量;半电池制作过程如下:取1.5gCNT及15g固含量为1.4%的CMC胶液匀浆,再称取0.09gSP,称取2.7g负极活性物质,加水9g搅拌,涂布350um,80℃烘2H;将上述负极片与锂箔片组成扣式电池,搁置至少12小时;测试方法如下:静置2h;0.1C倍率放电至5mv;0.05C倍率放电至5mv;0.02C倍率放电至5mv;0.01C倍率放电至5mv;0.1C倍率充电至2V;随后计算石墨可逆容量。在这里,石墨可逆容量=石墨脱锂容量/负极活性物质质量;倍率公式里的可逆容量已经归一化为克容量。Graphite reversible capacity (P2) means graphite reversible capacity refers to the first delithiation gram capacity of a half-battery made of graphite negative electrode sheet (here graphite negative electrode sheet refers to the negative active material only graphite); the half-battery production process is as follows: take 1.5g CNT and 15g solid content Homogenize 1.4% CMC glue solution, then weigh 0.09g SP, weigh 2.7g of negative active material, add 9g of water, stir, apply 350um, and bake at 80°C for 2H; combine the above negative electrode sheet and lithium foil to form a button battery. Leave it aside for at least 12 hours; the test method is as follows: leave it alone for 2 hours; discharge to 5mv at a 0.1C rate; discharge to 5mv at a 0.05C rate; discharge to 5mv at a 0.02C rate; discharge to 5mv at a 0.01C rate; charge to 2V at a 0.1C rate; then calculate Graphite reversible capacity. Here, graphite reversible capacity = graphite delithiation capacity/negative active material mass; the reversible capacity in the rate formula has been normalized to gram capacity.
硅含量(W1)表示硅的质量在硅和石墨的总质量中的占比;石墨含量(W2)表示石墨的质量在硅和石墨的总质量中的占比。The silicon content (W1) represents the proportion of the mass of silicon in the total mass of silicon and graphite; the graphite content (W2) represents the proportion of the mass of graphite in the total mass of silicon and graphite.
n1表示预嵌锂的硅占比,即嵌锂的硅的质量占所有硅的质量的比例;n1的值是根据长期经验而得到的值;其中,具体而言,n1低于0.3会导致硅嵌锂能力冗余,快充时间过长;n1高于0.7易导致硅单位时间嵌锂的硅占比过高,在硅颗粒内部产生较大的内应力。n2表示硅能够承受的最大电流密度时的充电倍率,是依据实际测试中硅到达3C倍率时,所对应的硅表面电流密度硅无法承受时的数值,这里无法承受是指硅表面电流密度过大,产生的内应力使硅颗粒破碎,加剧活性锂损失。C2表示预设快充时间所要求的最大倍率,是通过利用以下公式计算得到的:C2=60/预设快充时间,根据常规电池的快充时间为5~48分钟为预设快充时间计算得到。n1 represents the proportion of silicon pre-embedded with lithium, that is, the mass of lithium-embedded silicon accounts for the mass of all silicon; the value of n1 is a value obtained based on long-term experience; specifically, n1 lower than 0.3 will cause silicon The lithium-embedded capacity is redundant and the fast charging time is too long; n1 higher than 0.7 can easily lead to an excessively high proportion of silicon embedded with lithium per unit time, causing large internal stress inside the silicon particles. n2 represents the charging rate at the maximum current density that silicon can withstand. It is based on the value when silicon reaches 3C rate in actual testing and the corresponding silicon surface current density is unbearable. Unbearable here means that the silicon surface current density is too high. , the internal stress generated causes the silicon particles to break, exacerbating the loss of active lithium. C2 represents the maximum magnification required by the preset fast charge time, which is calculated by using the following formula: C2 = 60/preset fast charge time. The preset fast charge time is based on the fast charge time of a conventional battery being 5 to 48 minutes. calculated.
在本发明提供的含硅负极的锂电池的充电方法中,通过先采用较小充电倍率C1对锂电池进行充电,而接着再采用较大充电倍率C2对锂电池进行充电,有利于提高含硅负极中硅颗粒在充电过程中的稳定性,提高硅颗粒长期容量性能的发挥,降低锂电池在快充循环中的容量衰减率,提高锂电池的循环性能。In the charging method of the lithium battery containing silicon negative electrode provided by the present invention, by first charging the lithium battery with a smaller charging rate C1, and then using a larger charging rate C2 to charge the lithium battery, it is beneficial to increase the silicon content of the lithium battery. The stability of the silicon particles in the negative electrode during the charging process improves the long-term capacity performance of the silicon particles, reduces the capacity fading rate of lithium batteries in fast charging cycles, and improves the cycle performance of lithium batteries.
造成上述结果的原因在于,在硅/石墨复合负极中,在对锂电池进行充电时,硅会被先锂化,即锂离子会先嵌到硅颗粒中,而硅颗粒若在较大倍率下充电,硅颗粒的体积膨胀变化较大,且由于硅的锂离子传输动力学性能差引起的极化更大,因此在大倍率充电下硅的稳定性和容量发挥会变差,进而导致锂电池的循环性能变差。而在本发明中,首先采用较低的充电倍率对电池进行充电,可以使硅颗粒在初始阶段有充分的时间嵌锂,这样硅颗粒在初始阶段不会因为过大的充电倍率而承受过大的内部应力,有利于硅颗粒的缓慢膨胀,减少硅颗粒的膨胀变化体积,降低极化。而在使用较小的充电倍率对锂电池进行一定时间的充电后,这时一定含量的硅颗粒被预锂化到一定程度,即锂离子嵌在了一定含量的硅颗粒中,这时切换为较大的充电倍率,充电时剩余含量的硅颗粒和石墨颗粒被共同锂化,而石墨的锂离子传输动力学性能要比硅好,因此此时采用较大的充电倍率也不会对硅颗粒有过大的内部应力,有利于提高硅颗粒在整个充过程的稳定性,进而有利于硅颗粒的容量发挥,从而提升了硅/石墨负极材料的整体稳定性,优化了锂电池的循环性能。The reason for the above results is that in the silicon/graphite composite negative electrode, when charging the lithium battery, the silicon will be lithiated first, that is, the lithium ions will first be embedded into the silicon particles, and if the silicon particles are charged at a larger rate, During charging, the volume expansion of silicon particles changes greatly, and due to the poor lithium ion transport kinetics of silicon, the polarization is greater. Therefore, the stability and capacity of silicon will become worse under high-rate charging, which will lead to lithium batteries. cycle performance deteriorates. In the present invention, a lower charging rate is first used to charge the battery, which allows the silicon particles to have sufficient time to embed lithium in the initial stage. In this way, the silicon particles will not bear excessive stress due to an excessive charging rate in the initial stage. The internal stress is conducive to the slow expansion of silicon particles, reducing the expansion and change volume of silicon particles, and reducing polarization. After charging the lithium battery for a certain period of time using a smaller charging rate, a certain amount of silicon particles are prelithiated to a certain extent, that is, lithium ions are embedded in a certain amount of silicon particles, and then switch to At a larger charging rate, the remaining silicon particles and graphite particles are lithiated together during charging, and graphite has better lithium ion transport dynamics than silicon, so using a larger charging rate at this time will not damage the silicon particles. Excessive internal stress is conducive to improving the stability of the silicon particles throughout the charging process, which is conducive to the capacity of the silicon particles, thus improving the overall stability of the silicon/graphite anode material and optimizing the cycle performance of the lithium battery.
尽管现有技术中也有先采用小倍率后采用大倍率对锂电池进行充电,但现有技术中的充电方法大多数是针对大多数电池的充电,例如采用同一种充电方式对不同电池充电,但这样的充电方式其实并不能很好的适配于每一款电池。因为对于每一款不同的电池,制作电池时所采用的具体的材料会存在差别,进而,对于不同的电池,活性材料颗粒所承受的应力能力不同,所对应的C1也是不同的。如果对不同电池皆采用同一种充电方式,则会不可避免地对锂电池的充电性能、循环性能有一定的影响,长期采用不适配的充电方式会对造成锂电池的循环性能劣化得更快。而本发明通过控制影响C1的各种因素,对每个不同的锂电池都可确定一个最佳的C1值,可以为每个锂电池都提供一种个性化的充电方式,有利于锂电池容量的长期发挥,且有利于锂电池的循环性能。Although in the prior art, a small rate is first used and then a large rate is used to charge lithium batteries, most of the charging methods in the prior art are for charging most batteries. For example, the same charging method is used to charge different batteries, but In fact, this charging method is not well adapted to every battery. Because for each different battery, the specific materials used in making the battery will be different. Furthermore, for different batteries, the active material particles have different stress capabilities, and the corresponding C1 is also different. If the same charging method is used for different batteries, it will inevitably have a certain impact on the charging performance and cycle performance of the lithium battery. Long-term use of inappropriate charging methods will cause the cycle performance of the lithium battery to deteriorate faster. . By controlling various factors that affect C1, the present invention can determine an optimal C1 value for each different lithium battery, and can provide a personalized charging method for each lithium battery, which is beneficial to the capacity of the lithium battery. long-term performance, and is beneficial to the cycle performance of lithium batteries.
在上述关于第一充电阶段、第二充电阶段的充电倍率C1、C2的关系式中,C2的值通常与快充要求时间相关,为快充要求时间所需要的最大充电倍率,将C2与快充要求时间关联,一方面有利于根据客户需求设置不同的最大充电倍率,另一方面也有利于在保证硅/石墨负极材料的稳定性的同时,提高锂电池的充电效率。而C1除了与C2有关,还与预嵌锂的硅占比n1、硅能够承受的最大电流密度时的充电倍率n2、硅可逆容量P1、硅含量W1、石墨可逆容量P2以及石墨含量W2有关,而对于C1而言,硅可逆容量对其影响较大,因为硅可逆容量决定了硅颗粒脱嵌锂离子的动力学性能,而在硅/石墨复合负极中,硅颗粒相对于石墨颗粒而言离子迁移能力较差、且易体积膨胀引起硅颗粒破碎而导致极化加剧。因此,在硅/石墨复合负极中,使C1与C2满足上述关系式,有利于保证一开始的充电过程硅颗粒有合适的嵌锂速度,且使硅颗粒在较小的充电倍率C1下有较小的内部压力,不易产生破碎,有利于硅颗粒的稳定性,进而有利于硅颗粒长期容量性能的发挥,提高锂电池的循环性能。而其他因素n1、W1、P2、W2也均会在一定程度影响整个硅/石墨复合负极的脱嵌锂性能,对锂电池的循环性能较大。因此,将C1与上述影响因素关联,有利于充分考虑整个硅/石墨复合负极的脱嵌锂性能以及稳定性,更有利于得到更适合硅/石墨复合负极的锂电池的在第一充电阶段的小充电倍率C1。In the above relational expressions about the charging rates C1 and C2 of the first charging stage and the second charging stage, the value of C2 is usually related to the fast charging required time, which is the maximum charging rate required for the fast charging required time. C2 and fast charging The time correlation of charging requirements is beneficial to setting different maximum charging rates according to customer needs. On the other hand, it is also beneficial to improve the charging efficiency of lithium batteries while ensuring the stability of silicon/graphite anode materials. In addition to being related to C2, C1 is also related to the proportion of silicon pre-embedded with lithium n1, the charging rate n2 at the maximum current density that silicon can withstand, silicon reversible capacity P1, silicon content W1, graphite reversible capacity P2 and graphite content W2. For C1, the reversible capacity of silicon has a greater impact on it, because the reversible capacity of silicon determines the kinetic properties of silicon particles deintercalating lithium ions. In the silicon/graphite composite anode, silicon particles are more ion-free than graphite particles. The migration ability is poor, and volume expansion easily causes the silicon particles to break, resulting in increased polarization. Therefore, in the silicon/graphite composite negative electrode, making C1 and C2 satisfy the above relationship will help ensure that the silicon particles have an appropriate lithium insertion speed during the initial charging process, and make the silicon particles have a higher performance at a smaller charging rate C1. Small internal pressure is not easy to break, which is beneficial to the stability of silicon particles, which is beneficial to the long-term capacity performance of silicon particles and improves the cycle performance of lithium batteries. Other factors n1, W1, P2, and W2 will also affect the lithium deintercalation performance of the entire silicon/graphite composite negative electrode to a certain extent, which will greatly affect the cycle performance of the lithium battery. Therefore, associating C1 with the above influencing factors is conducive to fully considering the lithium deintercalation performance and stability of the entire silicon/graphite composite anode, and is more conducive to obtaining a lithium battery that is more suitable for the silicon/graphite composite anode in the first charging stage. Small charging rate C1.
另外,关于硅能够承受的最大电流密度时的充电倍率n2,其与硅含量W1相关,硅含量越高,n2越小。这是因为,硅含量越高,锂电池的首效越低,即单位质量的硅所能承受的最大电流密度越小。因此,硅含量决定了硅能够承受的最大电流密度时的充电倍率,硅含量对于整个锂电池体系的充电性能也有很重要的影响。In addition, regarding the charging rate n2 at the maximum current density that silicon can withstand, it is related to the silicon content W1. The higher the silicon content, the smaller n2 is. This is because the higher the silicon content, the lower the first efficiency of the lithium battery, that is, the smaller the maximum current density that unit mass of silicon can withstand. Therefore, the silicon content determines the charging rate at the maximum current density that silicon can withstand. The silicon content also has an important impact on the charging performance of the entire lithium battery system.
而关于第一充电阶段何时结束而切换到第二充电阶段,其是通过根据电池的SOC值来判断的。当在第一充电阶段中,SOC达到阈值b时,代表在硅/石墨复合电极中有一定含量的硅已经被嵌锂,锂电池的极化比较低,而剩余含量的硅与石墨可以同时被嵌锂,因此石墨颗粒分散了一部分的内部应力,即使在较大的充电倍率下,硅颗粒也不会破碎,有较好的稳定性。而阈值b与预嵌锂的硅占比n1、硅可逆容量P1、硅含量W1、石墨可逆容量P2以及石墨含量W2有关,这是考虑到硅/石墨复合负极的脱嵌锂性能以及稳定性能与这些因素有较大的相关性,而综合考虑这些因素,有利于判断硅/石墨复合负极承受应力的大小,得到更合适的阈值b,保证硅颗粒稳定性的同时,最大程度提高锂电池的充电效率。As for when the first charging phase ends and switches to the second charging phase, it is determined based on the SOC value of the battery. When the SOC reaches the threshold b in the first charging stage, it means that a certain content of silicon in the silicon/graphite composite electrode has been embedded with lithium. The polarization of the lithium battery is relatively low, and the remaining content of silicon and graphite can be lithium-ionized at the same time. Lithium is embedded, so the graphite particles disperse part of the internal stress. Even under larger charging rates, the silicon particles will not break and have good stability. The threshold b is related to the silicon ratio n1 of pre-intercalated lithium, silicon reversible capacity P1, silicon content W1, graphite reversible capacity P2 and graphite content W2. This is considering the lithium deintercalation performance and stability performance of the silicon/graphite composite anode. These factors are highly correlated, and taking these factors into consideration will help determine the stress the silicon/graphite composite negative electrode will bear, and obtain a more appropriate threshold b, which will ensure the stability of the silicon particles while maximizing the charging of the lithium battery. efficiency.
具体实施方式Detailed ways
本发明提供一种含硅负极的锂电池的充电方法,包括第一充电阶段和第二充电阶段;在第一充电阶段中,采用C1倍率充电;在第二充电阶段中,采用C2倍率充电;其中,C1和C2满足以下关系式:C1=n1×n2×C2×(P1×W1)/(P1×W1+P2×W2);其中,n1=0.3~0.7,n2=3.6-5×W1;C2=1.25~12;其中,在含硅负极中,负极活性物质包括硅和石墨,P1表示硅可逆容量,P2表示石墨可逆容量,W1表示硅含量,W2表示石墨含量;在锂电池的充电过程中,当第一充电阶段中锂电池的SOC值到达阈值a,第一充电阶段结束,切换为第二充电阶段;其中,a=n1×(P1×W1)/(P1×W1+P2×W2)。The invention provides a charging method for a lithium battery containing a silicon negative electrode, which includes a first charging stage and a second charging stage; in the first charging stage, C1 rate charging is used; in the second charging stage, C2 rate charging is used; Among them, C1 and C2 satisfy the following relationship: C1=n1×n2×C2×(P1×W1)/(P1×W1+P2×W2); among them, n1=0.3~0.7, n2=3.6-5×W1; C2=1.25~12; among them, in the silicon-containing negative electrode, the negative active material includes silicon and graphite, P1 represents the silicon reversible capacity, P2 represents the graphite reversible capacity, W1 represents the silicon content, and W2 represents the graphite content; during the charging process of lithium battery , when the SOC value of the lithium battery reaches the threshold a in the first charging stage, the first charging stage ends and switches to the second charging stage; where, a=n1×(P1×W1)/(P1×W1+P2×W2 ).
在本发明提供的含硅负极的锂电池的充电方法中,通过先采用较小充电倍率C1对锂电池进行充电,而接着再采用较大充电倍率C2对锂电池进行充电,有利于提高含硅负极中硅颗粒在充电过程中的稳定性,提高硅颗粒长期容量性能的发挥,降低锂电池在快充循环中的容量衰减率,提高锂电池的循环性能。In the charging method of the lithium battery containing silicon negative electrode provided by the present invention, by first charging the lithium battery with a smaller charging rate C1, and then using a larger charging rate C2 to charge the lithium battery, it is beneficial to increase the silicon content of the lithium battery. The stability of the silicon particles in the negative electrode during the charging process improves the long-term capacity performance of the silicon particles, reduces the capacity fading rate of lithium batteries in fast charging cycles, and improves the cycle performance of lithium batteries.
造成上述结果的原因在于,在硅/石墨复合负极中,在对锂电池进行充电时,硅会被先锂化,即锂离子会先嵌到硅颗粒中,而硅颗粒若在较大倍率下充电,硅颗粒的体积膨胀变化较大,且由于硅的锂离子传输动力学性能差引起的极化更大,因此在大倍率充电下硅的稳定性和容量发挥会变差,进而导致锂电池的循环性能变差。而在本发明中,首先采用较低的充电倍率对电池进行充电,可以使硅颗粒在初始阶段有充分的时间嵌锂,这样硅颗粒在初始阶段不会因为过大的充电倍率而承受过大的内部应力,有利于硅颗粒的缓慢膨胀,减少硅颗粒的膨胀变化体积,降低极化。而在使用较小的充电倍率对锂电池进行一定时间的充电后,这时一定含量的硅颗粒被预锂化到一定程度,即锂离子嵌在了一定含量的硅颗粒中,这时切换为较大的充电倍率,充电时剩余含量的硅颗粒和石墨颗粒被共同锂化,而石墨的锂离子传输动力学性能要比硅好,因此此时采用较大的充电倍率也不会对硅颗粒有过大的内部应力,有利于提高硅颗粒在整个充过程的稳定性,进而有利于硅颗粒的容量发挥,从而提升了硅/石墨负极材料的整体稳定性,优化了锂电池的循环性能。The reason for the above results is that in the silicon/graphite composite negative electrode, when charging the lithium battery, the silicon will be lithiated first, that is, the lithium ions will first be embedded into the silicon particles, and if the silicon particles are charged at a larger rate, During charging, the volume expansion of silicon particles changes greatly, and due to the poor lithium ion transport kinetics of silicon, the polarization is greater. Therefore, the stability and capacity of silicon will become worse under high-rate charging, which will lead to lithium batteries. cycle performance deteriorates. In the present invention, a lower charging rate is first used to charge the battery, which allows the silicon particles to have sufficient time to embed lithium in the initial stage. In this way, the silicon particles will not bear excessive stress due to an excessive charging rate in the initial stage. The internal stress is conducive to the slow expansion of silicon particles, reducing the expansion and change volume of silicon particles, and reducing polarization. After charging the lithium battery for a certain period of time using a smaller charging rate, a certain amount of silicon particles are prelithiated to a certain extent, that is, lithium ions are embedded in a certain amount of silicon particles, and then switch to At a larger charging rate, the remaining silicon particles and graphite particles are lithiated together during charging, and graphite has better lithium ion transport dynamics than silicon, so using a larger charging rate at this time will not damage the silicon particles. Excessive internal stress is conducive to improving the stability of the silicon particles throughout the charging process, which is conducive to the capacity of the silicon particles, thus improving the overall stability of the silicon/graphite anode material and optimizing the cycle performance of the lithium battery.
尽管现有技术中也有先采用小倍率后采用大倍率对锂电池进行充电,但现有技术中的充电方法大多数是针对大多数电池的充电,例如采用同一种充电方式对不同电池充电,但这样的充电方式其实并不能很好的适配于每一款电池。因为对于每一款不同的电池,制作电池时所采用的具体的材料会存在差别,进而,对于不同的电池,活性材料颗粒所承受的应力能力不同,所对应的C1也是不同的。如果对不同电池皆采用同一种充电方式,则会不可避免地对锂电池的充电性能、循环性能有一定的影响,长期采用不适配的充电方式会对造成锂电池的循环性能劣化得更快。而本发明通过控制影响C1的各种因素,对每个不同的锂电池都可确定一个最佳的C1值,可以为每个锂电池都提供一种个性化的充电方式,有利于锂电池容量的长期发挥,且有利于锂电池的循环性能。Although in the prior art, a small rate is first used and then a large rate is used to charge lithium batteries, most of the charging methods in the prior art are for charging most batteries. For example, the same charging method is used to charge different batteries, but In fact, this charging method is not well adapted to every battery. Because for each different battery, the specific materials used in making the battery will be different. Furthermore, for different batteries, the active material particles have different stress capabilities, and the corresponding C1 is also different. If the same charging method is used for different batteries, it will inevitably have a certain impact on the charging performance and cycle performance of the lithium battery. Long-term use of inappropriate charging methods will cause the cycle performance of the lithium battery to deteriorate faster. . By controlling various factors that affect C1, the present invention can determine an optimal C1 value for each different lithium battery, and can provide a personalized charging method for each lithium battery, which is beneficial to the capacity of the lithium battery. long-term performance, and is beneficial to the cycle performance of lithium batteries.
在上述关于第一充电阶段、第二充电阶段的充电倍率C1、C2的关系式中,C2的值通常与快充要求时间相关,为快充要求时间所需要的最大充电倍率,将C2与快充要求时间关联,一方面有利于根据客户需求设置不同的最大充电倍率,另一方面也有利于在保证硅/石墨负极材料的稳定性的同时,提高锂电池的充电效率。而C1除了与C2有关,还与预嵌锂的硅占比n1、硅能够承受的最大电流密度时的充电倍率n2、硅可逆容量P1、硅含量W1、石墨可逆容量P2以及石墨含量W2有关,而对于C1而言,硅可逆容量对其影响较大,因为硅可逆容量决定了硅颗粒脱嵌锂离子的动力学性能,而在硅/石墨复合负极中,硅颗粒相对于石墨颗粒而言离子迁移能力较差、且易体积膨胀引起硅颗粒破碎而导致极化加剧。因此,在硅/石墨复合负极中,使C1与C2满足上述关系式,有利于保证一开始的充电过程硅颗粒有合适的嵌锂速度,且使硅颗粒在较小的充电倍率C1下有较小的内部压力,不易产生破碎,有利于硅颗粒的稳定性,进而有利于硅颗粒长期容量性能的发挥,提高锂电池的循环性能。而其他因素n1、W1、P2、W2也均会在一定程度影响整个硅/石墨复合负极的脱嵌锂性能,对锂电池的循环性能较大。因此,将C1与上述影响因素关联,有利于充分考虑整个硅/石墨复合负极的脱嵌锂性能以及稳定性,更有利于得到更适合硅/石墨复合负极的锂电池的在第一充电阶段的小充电倍率C1。In the above relational expressions about the charging rates C1 and C2 of the first charging stage and the second charging stage, the value of C2 is usually related to the fast charging required time, which is the maximum charging rate required for the fast charging required time. C2 and fast charging The time correlation of charging requirements is beneficial to setting different maximum charging rates according to customer needs. On the other hand, it is also beneficial to improve the charging efficiency of lithium batteries while ensuring the stability of silicon/graphite anode materials. In addition to being related to C2, C1 is also related to the proportion of silicon pre-embedded with lithium n1, the charging rate n2 at the maximum current density that silicon can withstand, silicon reversible capacity P1, silicon content W1, graphite reversible capacity P2 and graphite content W2. For C1, the reversible capacity of silicon has a greater impact on it, because the reversible capacity of silicon determines the kinetic properties of silicon particles deintercalating lithium ions. In the silicon/graphite composite anode, silicon particles are more ion-free than graphite particles. The migration ability is poor, and volume expansion easily causes the silicon particles to break, resulting in increased polarization. Therefore, in the silicon/graphite composite negative electrode, making C1 and C2 satisfy the above relationship will help ensure that the silicon particles have an appropriate lithium insertion speed during the initial charging process, and make the silicon particles have a higher performance at a smaller charging rate C1. Small internal pressure is not easy to break, which is beneficial to the stability of silicon particles, which is beneficial to the long-term capacity performance of silicon particles and improves the cycle performance of lithium batteries. Other factors n1, W1, P2, and W2 will also affect the lithium deintercalation performance of the entire silicon/graphite composite negative electrode to a certain extent, which will greatly affect the cycle performance of the lithium battery. Therefore, associating C1 with the above influencing factors is conducive to fully considering the lithium deintercalation performance and stability of the entire silicon/graphite composite anode, and is more conducive to obtaining a lithium battery that is more suitable for the silicon/graphite composite anode in the first charging stage. Small charging rate C1.
另外,关于硅能够承受的最大电流密度时的充电倍率n2,其与硅含量W1相关,硅含量越高,n2越小。这是因为,硅含量越高,锂电池的首效越低,即单位质量的硅所能承受的最大电流密度越小。因此,硅含量决定了硅能够承受的最大电流密度时的充电倍率,硅含量对于整个锂电池体系的充电性能也有很重要的影响。In addition, regarding the charging rate n2 at the maximum current density that silicon can withstand, it is related to the silicon content W1. The higher the silicon content, the smaller n2 is. This is because the higher the silicon content, the lower the first efficiency of the lithium battery, that is, the smaller the maximum current density that unit mass of silicon can withstand. Therefore, the silicon content determines the charging rate at the maximum current density that silicon can withstand. The silicon content also has an important impact on the charging performance of the entire lithium battery system.
而关于第一充电阶段何时结束而切换到第二充电阶段,其是通过根据电池的SOC值来判断的。当在第一充电阶段中,SOC达到阈值b时,代表在硅/石墨复合电极中有一定含量的硅已经被嵌锂,锂电池的极化比较低,而剩余含量的硅与石墨可以同时被嵌锂,因此石墨颗粒分散了一部分的内部应力,即使在较大的充电倍率下,硅颗粒也不会破碎,有较好的稳定性。而阈值b与预嵌锂的硅占比n1、硅可逆容量P1、硅含量W1、石墨可逆容量P2以及石墨含量W2有关,这是考虑到硅/石墨复合负极的脱嵌锂性能以及稳定性能与这些因素有较大的相关性,而综合考虑这些因素,有利于判断硅/石墨复合负极承受应力的大小,得到更合适的阈值b,保证硅颗粒稳定性的同时,最大程度提高锂电池的充电效率。As for when the first charging phase ends and switches to the second charging phase, it is determined based on the SOC value of the battery. When the SOC reaches the threshold b in the first charging stage, it means that a certain content of silicon in the silicon/graphite composite electrode has been embedded with lithium. The polarization of the lithium battery is relatively low, and the remaining content of silicon and graphite can be lithium-ionized at the same time. Lithium is embedded, so the graphite particles disperse part of the internal stress. Even under larger charging rates, the silicon particles will not break and have good stability. The threshold b is related to the silicon ratio n1 of pre-intercalated lithium, silicon reversible capacity P1, silicon content W1, graphite reversible capacity P2 and graphite content W2. This is considering the lithium deintercalation performance and stability performance of the silicon/graphite composite anode. These factors are highly correlated, and taking these factors into consideration will help determine the stress the silicon/graphite composite negative electrode will bear, and obtain a more appropriate threshold b, which will ensure the stability of the silicon particles while maximizing the charging of the lithium battery. efficiency.
优选地,W1=0.01~0.5,W2=1-W1,n2=1.1~3.55。Preferably, W1=0.01~0.5, W2=1-W1, n2=1.1~3.55.
优选地,P1=1500~2000mAh/g,P2=330~370mAh/g。Preferably, P1=1500~2000mAh/g, P2=330~370mAh/g.
优选地,n1=0.4~0.6。Preferably, n1=0.4~0.6.
优选地,n2=2.5~3.55。Preferably, n2=2.5~3.55.
当n1或者n2分别在上述数值范围内时,更有利于调控C1的值更适合第一充电阶段,既可以保证硅颗粒在被预锂化时不被过大的内部应力致使破碎,又能保证硅可以较快地被预锂化,缩短第一阶段充电时间,进而提高整个充电过程的充电效率。When n1 or n2 are respectively within the above numerical range, it is more conducive to adjust the value of C1 to be more suitable for the first charging stage, which can not only ensure that the silicon particles are not broken by excessive internal stress when being prelithiated, but also ensure that Silicon can be prelithiated faster, shortening the first-stage charging time and thus improving the charging efficiency of the entire charging process.
优选地,在第一充电阶段中,锂电池起始充电的SOC<20%。保证在第一充电阶段中,锂电池起始充电的SOC符合上述条件,能够保证在第一充电阶段的过程中锂离子能够全部嵌在硅颗粒中,保证有充分比例的硅颗粒被预锂化,保证进入到第二充电阶段时锂离子能够同时被剩余硅颗粒和石墨颗粒嵌锂,使在大充电倍率下石墨颗粒能有效的分担部分内部应力,避免硅颗粒易破碎,提高硅颗粒的稳定性。Preferably, in the first charging stage, the SOC of the initial charge of the lithium battery is <20%. Ensure that in the first charging stage, the SOC of the initial charging of the lithium battery meets the above conditions, ensuring that all lithium ions can be embedded in the silicon particles during the first charging stage, and ensuring that a sufficient proportion of the silicon particles are prelithiated. , ensuring that when entering the second charging stage, lithium ions can be embedded in lithium by the remaining silicon particles and graphite particles at the same time, so that the graphite particles can effectively share part of the internal stress under large charging rates, avoid the easy breakage of the silicon particles, and improve the stability of the silicon particles. sex.
优选地,在第一充电阶段前,还包括预先充电阶段;当预先充电阶段结束,锂电池的SOC<10%。Preferably, before the first charging stage, a pre-charging stage is also included; when the pre-charging stage ends, the SOC of the lithium battery is <10%.
优选地,在第一充电阶段中,含硅负极表面的电流密度的峰值不大于9.2mA·cm-2。此处含硅负极表面的电流密度,表示单位面密度负极所能承受的电流。保证含硅负极表面的电流密度符合上述条件,可以保证含硅负极中的颗粒不易破碎,有利于保证含硅负极在充电过程中的稳定性,提高锂电池的循环稳定性。Preferably, in the first charging stage, the peak value of the current density on the surface of the silicon-containing negative electrode is no more than 9.2 mA·cm -2 . The current density on the surface of the silicon-containing negative electrode here represents the current that the negative electrode can withstand per unit area density. Ensuring that the current density on the surface of the silicon-containing negative electrode meets the above conditions can ensure that the particles in the silicon-containing negative electrode are not easily broken, which is beneficial to ensuring the stability of the silicon-containing negative electrode during the charging process and improving the cycle stability of lithium batteries.
优选地,在第二充电阶段中,含硅负极表面的电流密度的峰值不小于bmA·cm-2,b=4.6×C1。使第二充电阶段含硅负极表面的电流密度的峰值满足上述条件,不但能保证锂电池能快速充电,提高充电效率,而且有利于含硅负极在整个充电过程又较好的稳定性,有利于容量的发挥和锂电池的循环性能。Preferably, in the second charging stage, the peak value of the current density on the surface of the silicon-containing negative electrode is not less than bmA·cm -2 , b=4.6×C1. Making the peak current density on the surface of the silicon-containing anode meet the above conditions in the second charging stage not only ensures that the lithium battery can be charged quickly and improves the charging efficiency, but also facilitates the stability of the silicon-containing anode during the entire charging process. Capacity development and cycle performance of lithium batteries.
优选地,C1=0.2~2C。使C1在上述数值范围,有利于保证第一充电过程中硅基负极中硅颗粒的稳定性,有利于硅长期容量性能的发挥。Preferably, C1=0.2~2C. Keeping C1 within the above numerical range is beneficial to ensuring the stability of the silicon particles in the silicon-based negative electrode during the first charging process, and is beneficial to the long-term capacity performance of silicon.
优选地,在含硅负极中,W1=0.1~0.3。保证含硅负极中硅的含量在上述范围内,一方面,避免过少的硅含量不能有效的提升锂电池的容量,另一方面,也能避免过多的硅含量会导致硅/石墨复合负极整体的膨胀率变大,劣化锂电池的循环性能。Preferably, in the silicon-containing negative electrode, W1=0.1~0.3. Ensure that the silicon content in the silicon-containing negative electrode is within the above range. On the one hand, it can avoid that too little silicon content cannot effectively increase the capacity of lithium batteries. On the other hand, it can also avoid that too much silicon content can cause silicon/graphite composite negative electrodes. The overall expansion rate increases, deteriorating the cycle performance of lithium batteries.
优选地,在第二充电阶段,充电倍率按照最高倍率C2依次降阶。Preferably, in the second charging stage, the charging rate is sequentially reduced according to the highest rate C2.
优选地,第二充电阶段结束,锂电池的SOC不低于80%。Preferably, at the end of the second charging stage, the SOC of the lithium battery is not less than 80%.
优选地,在上述含硅负极的锂电池的充电方法中,还包括第三充电阶段;在第三充电阶段中,锂电池起始的SOC不低于80%。Preferably, the above charging method for a lithium battery containing a silicon negative electrode further includes a third charging stage; in the third charging stage, the initial SOC of the lithium battery is not less than 80%.
优选地,锂电池还包括正极,正极包括正极活性物质,正极活性物质包括镍钴锰三元材料。Preferably, the lithium battery further includes a positive electrode, the positive electrode includes a positive electrode active material, and the positive electrode active material includes a nickel-cobalt-manganese ternary material.
根据本发明的另一个方面,提高一种锂电池的充电装置,采用上述含硅负极的锂电池的充电方法。According to another aspect of the present invention, a lithium battery charging device is provided, which adopts the above-mentioned charging method of a lithium battery containing a silicon negative electrode.
为了使本技术领域的人员更好地理解本发明方案,下面将对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分的实施例,而不是全部的实施例。In order to enable those skilled in the art to better understand the solutions of the present invention, the technical solutions in the embodiments of the present invention will be clearly and completely described below. Obviously, the described embodiments are only embodiments of a part of the present invention, rather than All examples.
以下实施例和对比例主要是通过选取不同的锂电池进行充电的,且通过控制每个实施例和对比例中影响充电的参数,探究本发明所提供的充电方法对锂电池充电时间以及循环性能的影响。The following examples and comparative examples are mainly based on selecting different lithium batteries for charging, and by controlling the parameters that affect charging in each example and comparative example, the charging method provided by the present invention is explored on the charging time and cycle performance of lithium batteries. Impact.
实施例1Example 1
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.236,预嵌锂的硅占比n1为0.7,硅能够承受的最大电流密度时的充电倍率n2为2.7,第一充电阶段的C1为1.9C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.236, the proportion of silicon pre-embedded with lithium n1 is 0.7, the charging rate n2 at the maximum current density that silicon can withstand is 2.7, C1 in the first charging stage is 1.9C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.9C将锂电池充电至23.6%SOC;(2) First charging stage: then charge the lithium battery to 23.6% SOC at 1.9C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作如下:①以3C从23.6%SOC充电至40%SOC;②以2.8C从40%SOC充电至42%SOC;③以2.6C从42%SOC充电至45%SOC;④以2.4C从45%SOC充电至50%SOC;⑤以2.2C从50%SOC充电至60%SOC;⑥以2.0C从60%SOC充电至65%SOC;⑦以1.8C从65%SOC充电至68%SOC;⑧以1.6C从68%SOC充电至70%SOC;⑨以1.4C从70%SOC充电至80%SOC。Among them, in the second charging stage, the specific charging operations of the lithium battery are as follows: ① charge from 23.6% SOC to 40% SOC at 3C; ② charge from 40% SOC to 42% SOC at 2.8C; ③ charge from 42% SOC to 42% SOC at 2.6C % SOC to 45% SOC; ④ Charge from 45% SOC to 50% SOC at 2.4C; ⑤ Charge from 50% SOC to 60% SOC at 2.2C; ⑥ Charge from 60% SOC to 65% SOC at 2.0C; ⑦ Charge from 65% SOC to 68% SOC at 1.8C; ⑧ Charge from 68% SOC to 70% SOC at 1.6C; ⑨ Charge from 70% SOC to 80% SOC at 1.4C.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
按照如下步骤对锂电池进行循环性能测试:Follow the steps below to perform cycle performance testing on lithium batteries:
步骤1:在25℃下将锂电池静置2h,使其达到热平衡;Step 1: Let the lithium battery stand for 2 hours at 25°C to allow it to reach thermal equilibrium;
步骤2:将锂电池以1/3C放电至2.8V;Step 2: Discharge the lithium battery to 2.8V at 1/3C;
步骤3:将锂电池静置30min;Step 3: Leave the lithium battery for 30 minutes;
步骤4:以上述充电方法(参考2.锂电池的充电)对锂电池进行充电;Step 4: Charge the lithium battery using the above charging method (refer to 2. Charging of lithium batteries);
步骤5:将锂电池静置10min;Step 5: Let the lithium battery stand for 10 minutes;
步骤6:重复步骤2~5至电池健康状态到80%SOH。Step 6: Repeat steps 2 to 5 until the battery health status reaches 80% SOH.
实施例2Example 2
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.202,预嵌锂的硅占比n1为0.6,硅能够承受的最大电流密度时的充电倍率n2为2.7,第一充电阶段的C1为1.6C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.202, the proportion of silicon pre-embedded with lithium n1 is 0.6, the charging rate n2 at the maximum current density that silicon can withstand is 2.7, C1 in the first charging stage is 1.6C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.6C将锂电池充电至20.2%SOC;(2) First charging stage: then charge the lithium battery to 20.2% SOC at 1.6C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从20.2%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 20.2% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例3Example 3
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.135,预嵌锂的硅占比n1为0.4,硅能够承受的最大电流密度时的充电倍率n2为2.7,第一充电阶段的C1为1.1C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.135, the proportion of silicon pre-embedded with lithium n1 is 0.4, the charging rate n2 at the maximum current density that silicon can withstand is 2.7, C1 in the first charging stage is 1.1C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.1C将锂电池充电至13.5%SOC;(2) First charging stage: Then charge the lithium battery to 13.5% SOC at 1.1C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从13.5%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 13.5% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例4Example 4
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.101,预嵌锂的硅占比n1为0.3,硅能够承受的最大电流密度时的充电倍率n2为2.7,第一充电阶段的C1为0.8C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.101, the proportion of silicon pre-embedded with lithium n1 is 0.3, the charging rate n2 at the maximum current density that silicon can withstand is 2.7, C1 in the first charging stage is 0.8C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以0.8C将锂电池充电至10.1%SOC;(2) First charging stage: then charge the lithium battery to 10.1% SOC at 0.8C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从10.1%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 10.1% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例5Example 5
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.168,预嵌锂的硅占比n1为0.5,硅能够承受的最大电流密度时的充电倍率n2为3.55,第一充电阶段的C1为1.8C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.168, the proportion of silicon pre-embedded with lithium n1 is 0.5, the charging rate n2 at the maximum current density that silicon can withstand is 3.55, C1 in the first charging stage is 1.8C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.8C将锂电池充电至16.8%SOC;(2) First charging stage: then charge the lithium battery to 16.8% SOC at 1.8C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从16.8%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 16.8% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例6Example 6
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.168,预嵌锂的硅占比n1为0.5,硅能够承受的最大电流密度时的充电倍率n2为3.5,第一充电阶段的C1为1.78C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.168, the proportion of silicon pre-embedded with lithium n1 is 0.5, the charging rate n2 at the maximum current density that silicon can withstand is 3.5, the C1 of the first charging stage is 1.78C, and the C2 setting of the second charging stage for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.78C将锂电池充电至16.8%SOC;(2) First charging stage: Then charge the lithium battery to 16.8% SOC at 1.78C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从16.8%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 16.8% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例7Example 7
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.168,预嵌锂的硅占比n1为0.5,硅能够承受的最大电流密度时的充电倍率n2为2.5,第一充电阶段的C1为1.3C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.168, the proportion of silicon pre-embedded with lithium n1 is 0.5, the charging rate n2 at the maximum current density that silicon can withstand is 2.5, C1 in the first charging stage is 1.3C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.3C将锂电池充电至16.8%SOC;(2) First charging stage: then charge the lithium battery to 16.8% SOC at 1.3C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从16.8%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 16.8% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例8Example 8
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.168,预嵌锂的硅占比n1为0.5,硅能够承受的最大电流密度时的充电倍率n2为1.1,第一充电阶段的C1为0.6C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.168, the proportion of silicon pre-embedded with lithium n1 is 0.5, the charging rate n2 at the maximum current density that silicon can withstand is 1.1, C1 in the first charging stage is 0.6C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以0.6C将锂电池充电至16.8%SOC;(2) First charging stage: then charge the lithium battery to 16.8% SOC at 0.6C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中的降阶情况与实施例1一致。Among them, in the second charging stage, the downgrading situation in the specific charging operation of the lithium battery is consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例9Example 9
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.15,石墨含量W2为0.85,阈值a为0.237,预嵌锂的硅占比n1为0.7,硅能够承受的最大电流密度时的充电倍率n2为2.7,第一充电阶段的C1为1.9C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.15, and the graphite content W2 is 0.85, the threshold a is 0.237, the proportion of silicon pre-embedded with lithium n1 is 0.7, the charging rate n2 at the maximum current density that silicon can withstand is 2.7, C1 in the first charging stage is 1.9C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.9C将锂电池充电至23.7%SOC;(2) First charging stage: then charge the lithium battery to 23.7% SOC at 1.9C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为0.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 0.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从23.7%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 23.7% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例10Example 10
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.168,预嵌锂的硅占比n1为0.5,硅能够承受的最大电流密度时的充电倍率n2为3.7,第一充电阶段的C1为0.4C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.168, the proportion of silicon pre-embedded with lithium n1 is 0.5, the charging rate n2 at the maximum current density that silicon can withstand is 3.7, C1 in the first charging stage is 0.4C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.9C将锂电池充电至16.8%SOC;(2) First charging stage: then charge the lithium battery to 16.8% SOC at 1.9C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为0.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 0.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从16.8%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 16.8% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例11Example 11
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实施例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.168,预嵌锂的硅占比n1为0.5,硅能够承受的最大电流密度时的充电倍率n2为0.8,第一充电阶段的C1为1.9C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this embodiment are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9, the threshold a is 0.168, the proportion of silicon pre-embedded with lithium n1 is 0.5, the charging rate n2 at the maximum current density that silicon can withstand is 0.8, C1 in the first charging stage is 1.9C, and C2 in the second charging stage is set for 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以0.4C将锂电池充电至16.8%SOC;(2) First charging stage: then charge the lithium battery to 16.8% SOC at 0.4C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为1.4C;(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 1.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从16.8%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 16.8% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
实施例12Example 12
1.锂电池的相关参数1. Relevant parameters of lithium battery
本实施例中的锂电池的相关参数除了C2与实施例1不一致,其余参数与实施例1一致,其中,C2设置为2C。The relevant parameters of the lithium battery in this embodiment are consistent with those in Embodiment 1 except for C2, where C2 is set to 2C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以1.9C将锂电池充电至23.6%SOC;(2) First charging stage: then charge the lithium battery to 23.6% SOC at 1.9C;
(3)第二充电阶段:接着以2C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为0.4C;(3) Second charging stage: Then use 2C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 0.4C;
(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作如下:①以2C从23.6%SOC充电至65%SOC;②以1.8C从65%SOC充电至68%SOC;③以1.6C从68%SOC充电至70%SOC;④以1.4C从70%SOC充电至80%SOC;⑤以0.33C从80%SOC充电至100%SOC。Among them, in the second charging stage, the specific charging operations of the lithium battery are as follows: ① Charge from 23.6% SOC to 65% SOC at 2C; ② Charge from 65% SOC to 68% SOC at 1.8C; ③ From 68% to 68% SOC at 1.6C % SOC charging to 70% SOC; ④ charging from 70% SOC to 80% SOC at 1.4C; ⑤ charging from 80% SOC to 100% SOC at 0.33C.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本实施例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this example is consistent with Example 1.
对比例1Comparative example 1
1.锂电池的相关参数1. Relevant parameters of lithium battery
本对比例直接用大倍率C2给锂电池充电,因此没有小倍率C1的第一充电阶段,即锂电池经历预先充电阶段后直接进入到第二充电阶段,第二充电阶段的C2设置为3C。且本对比例中锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9。This comparison example directly uses high-rate C2 to charge the lithium battery, so there is no first charging stage with small-rate C1. That is, the lithium battery directly enters the second charging stage after going through the pre-charging stage, and C2 in the second charging stage is set to 3C. The relevant parameters of the lithium battery in this comparative example are as follows: the reversible silicon content P1 is 1600mAh·g -1 , the reversible graphite content P2 is 350mAh·g -1 , the silicon content W1 is 0.1, and the graphite content W2 is 0.9.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80% SOC,第二充电阶段的最终截止充电倍率为0.4C;(2) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a step-down manner of reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 0.4C;
(3)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(3) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作如下:①以3C从5%SOC充电至40%SOC;②以2.8C从40%SOC充电至42%SOC;③以2.6C从42%SOC充电至45%SOC;④以2.4C从45%SOC充电至50%SOC;⑤以2.2C从50%SOC充电至60%SOC;⑥以2.0C从60%SOC充电至65%SOC;⑦以1.8C从65%SOC充电至68%SOC;⑧以1.6C从68%SOC充电至70%SOC;⑨以1.4C从70%SOC充电至80%SOC。Among them, in the second charging stage, the specific charging operations of the lithium battery are as follows: ① charge from 5% SOC to 40% SOC at 3C; ② charge from 40% SOC to 42% SOC at 2.8C; ③ charge from 42% SOC to 42% SOC at 2.6C. % SOC to 45% SOC; ④ Charge from 45% SOC to 50% SOC at 2.4C; ⑤ Charge from 50% SOC to 60% SOC at 2.2C; ⑥ Charge from 60% SOC to 65% SOC at 2.0C; ⑦ Charge from 65% SOC to 68% SOC at 1.8C; ⑧ Charge from 68% SOC to 70% SOC at 1.6C; ⑨ Charge from 70% SOC to 80% SOC at 1.4C.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本对比例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this comparative example is consistent with Example 1.
对比例2Comparative example 2
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实对比例中的锂电池的相关参数如下:硅可逆含量P1为1600mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.303,预嵌锂的硅占比n1为0.9,硅能够承受的最大电流密度时的充电倍率n2为3,第一充电阶段的C1为2.7C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this comparative example are as follows: silicon reversible content P1 is 1600mAh·g -1 , graphite reversible content P2 is 350mAh·g -1 , silicon content W1 is 0.1, graphite content W2 is 0.9, the threshold a is 0.303, the proportion of silicon pre-embedded with lithium n1 is 0.9, the charging rate n2 at the maximum current density that silicon can withstand is 3, C1 in the first charging stage is 2.7C, and C2 in the second charging stage Set to 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以2.7C将锂电池充电至30.3%SOC;(2) First charging stage: then charge the lithium battery to 30.3% SOC at 2.7C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80%SOC,第二充电阶段的最终截止充电倍率为0.4C;(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a reduced-step manner by reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 0.4C; ( 4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从30.3%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 30.3% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本对比例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this comparative example is consistent with Example 1.
对比例3Comparative example 3
1.锂电池的相关参数1. Relevant parameters of lithium battery
通过相关测试和计算,本实对比例中的锂电池的相关参数如下:硅可逆含量P1为1600 mAh·g-1,石墨可逆含量P2为350mAh·g-1,硅含量W1为0.1,石墨含量W2为0.9,阈值a为0.067,预嵌锂的硅占比n1为0.2,硅能够承受的最大电流密度时的充电倍率n2为3,第一充电阶段的C1为0.6C,第二充电阶段的C2设置为3C。Through relevant tests and calculations, the relevant parameters of the lithium battery in this comparative example are as follows: silicon reversible content P1 is 1600 mAh·g -1 , graphite reversible content P2 is 350mAh·g -1 , silicon content W1 is 0.1, graphite content W2 is 0.9, the threshold a is 0.067, the proportion of silicon pre-embedded with lithium n1 is 0.2, the charging rate n2 at the maximum current density that silicon can withstand is 3, C1 in the first charging stage is 0.6C, and C1 in the second charging stage C2 is set to 3C.
2.锂电池的充电2.Charging of lithium battery
按照如下步骤对锂电池进行充电:Follow the steps below to charge the lithium battery:
(1)预先充电阶段:以0.33C将锂电池充电至5%SOC;(1) Pre-charging stage: charge the lithium battery to 5% SOC at 0.33C;
(2)第一充电阶段:接着以0.6C将锂电池充电至6.7%SOC;(2) First charging stage: then charge the lithium battery to 6.7% SOC at 0.6C;
(3)第二充电阶段:接着以3C为最高充电倍率,且以每次减少0.2C的降阶形式对锂电池充电至80%SOC,第二充电阶段的最终截止充电倍率为0.4C;(4)第三充电阶段:最后以0.33C将锂电池充电至100%SOC。(3) Second charging stage: Then use 3C as the highest charging rate, and charge the lithium battery to 80% SOC in a reduced-step manner by reducing 0.2C each time. The final cut-off charging rate of the second charging stage is 0.4C; ( 4) The third charging stage: Finally, charge the lithium battery to 100% SOC at 0.33C.
其中,在第二充电阶段,对锂电池的具体充电操作中,①中以3C从6.7%SOC充电至40%SOC,其余的降阶情况与实施例1一致。Among them, in the second charging stage, in the specific charging operation of the lithium battery, 3C is used to charge from 6.7% SOC to 40% SOC in ①, and the remaining step reduction conditions are consistent with Embodiment 1.
另外,以首次充电所需时间为充电时长,记录充电时长。In addition, the charging time is taken as the first charging time, and the charging time is recorded.
3.锂电池的循环测试过程3. Lithium battery cycle test process
本对比例中对锂电池的循环性能测试与实施例1一致。The cycle performance test of the lithium battery in this comparative example is consistent with Example 1.
测试结果Test Results
如下表1是关于上述实施例和对比例中电池的相关参数和循环性能测试结果。Table 1 below is about the relevant parameters and cycle performance test results of the batteries in the above embodiments and comparative examples.
表1实施例和对比例中电池的相关参数和循环性能测试结果Table 1 Relevant parameters and cycle performance test results of batteries in Examples and Comparative Examples
由表1可以看出,利用本发明的充电方法对锂电池进行充电,可以既实现锂电池的快速充电,又可以实现使锂电池具有较好的循环性能,可参考表1中的数据。这是因为本发明中的充电方法中,其通过先采用较小充电倍率C1对锂电池进行充电,而接着再采用较大充电倍率C2对锂电池进行充电,有利于提高含硅负极中硅颗粒在充电过程中的稳定性,使硅颗粒不易破碎,提高硅颗粒长期容量性能的发挥,降低锂电池在快充循环中的容量衰减率,有利于在减少充电时间的同时提高锂电池的循环性能。且本发明中的充电方法通过控制影响C1的各种因素,对每个不同的锂电池都可确定一个最佳的C1值,可以为每个锂电池都提供一种个性化的充电方式,有利于锂电池容量的长期发挥,且有利于锂电池的循环性能。It can be seen from Table 1 that charging lithium batteries using the charging method of the present invention can not only achieve rapid charging of lithium batteries, but also achieve better cycle performance of lithium batteries. Please refer to the data in Table 1. This is because in the charging method of the present invention, by first charging the lithium battery with a smaller charging rate C1, and then using a larger charging rate C2 to charge the lithium battery, it is beneficial to increase the silicon particles in the silicon-containing negative electrode. The stability during the charging process makes the silicon particles less likely to break, improves the long-term capacity performance of the silicon particles, and reduces the capacity fading rate of lithium batteries in fast charging cycles, which is beneficial to reducing charging time while improving the cycle performance of lithium batteries. . Moreover, the charging method in the present invention can determine an optimal C1 value for each different lithium battery by controlling various factors that affect C1, and can provide a personalized charging method for each lithium battery. It is beneficial to the long-term performance of lithium battery capacity and the cycle performance of lithium batteries.
从实施例1~6中可以看出,n1的取值对锂电池的充电时间与循环性能的平衡是有影响的,当n1在0.4~0.6之间时,更有利于锂电池充电时间与循环性能的平衡,在实现更短的充电时间的同时能够进一步优化电池的循环性能。It can be seen from Examples 1 to 6 that the value of n1 has an impact on the balance between charging time and cycle performance of lithium batteries. When n1 is between 0.4 and 0.6, it is more beneficial to the charging time and cycle performance of lithium batteries. The balance of performance can further optimize the cycle performance of the battery while achieving shorter charging time.
从实施例5、6、7、8中可以看出,n2的取值对锂电池的充电时间与循环性能的平衡也是有一定的影响的,当n2在2.5~3.55之间时,更有利于锂电池充电时间与循环性能的平衡。而对比例1中直接采用大倍率C2对锂电池进行充电,硅颗粒一下子受到的应力过大,造成硅颗粒容易破碎,稳定性下降,因此劣化了锂电池的循环性能。对比例2、3中n1的值不在0.3~0.7之间,因此锂电池的循环性能或者充电时间都有一定的劣化,这说明,保持n1在合适的范围内,对锂电池充电时间与循环性能的平衡有重要的意义。It can be seen from Examples 5, 6, 7, and 8 that the value of n2 also has a certain impact on the balance between charging time and cycle performance of lithium batteries. When n2 is between 2.5 and 3.55, it is more beneficial. Balancing charging time and cycle performance of lithium batteries. In Comparative Example 1, high-rate C2 is directly used to charge the lithium battery. The silicon particles are suddenly subjected to excessive stress, causing the silicon particles to be easily broken and the stability to be reduced, thus degrading the cycle performance of the lithium battery. In Comparative Examples 2 and 3, the value of n1 is not between 0.3 and 0.7, so the cycle performance or charging time of the lithium battery has deteriorated to a certain extent. This shows that keeping n1 within the appropriate range will improve the charging time and cycle performance of the lithium battery. The balance is of great significance.
以上实施例仅用以说明本发明的技术方案而非对本发明保护范围的限制,尽管参照上述实施例对本发明进行了详细的说明,所属领域的普通技术人员应当理解,可以对本发明的技术方案进行修改或者等同替换,但这些修改或替换均在本发明的保护范围之内。The above embodiments are only used to illustrate the technical solutions of the present invention and do not limit the protection scope of the present invention. Although the present invention has been described in detail with reference to the above embodiments, those of ordinary skill in the art should understand that the technical solutions of the present invention can be carried out. modifications or equivalent substitutions, but these modifications or substitutions are within the protection scope of the present invention.
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Citations (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000203818A (en) * | 1999-01-13 | 2000-07-25 | Hitachi Chem Co Ltd | Composite carbon particle, its production, negative pole material, negative pole for lithium secondary battery or cell and lithium secondary battery or cell |
KR101511694B1 (en) * | 2013-11-29 | 2015-04-24 | 한화케미칼 주식회사 | Anode active material of lithium rechargeable battery and process for preparing the same |
CN106450246A (en) * | 2016-12-28 | 2017-02-22 | 江西正拓新能源科技股份有限公司 | Porous silicon-carbon composite material for lithium ion battery and preparation method of material |
US20170194672A1 (en) * | 2015-12-30 | 2017-07-06 | Nissan North America, Inc. | High current treatment for lithium ion batteries having metal based anodes |
EP3297070A1 (en) * | 2016-09-19 | 2018-03-21 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Lithium battery comprising a negative electrode with improved service life |
DE102018109698A1 (en) * | 2017-04-25 | 2018-10-25 | GM Global Technology Operations LLC | Method and apparatus for evaluating battery cells containing materials that have a voltage hysteresis |
CN108808140A (en) * | 2018-04-26 | 2018-11-13 | 江西优特汽车技术有限公司 | A kind of power battery charging management method |
CN111900352A (en) * | 2020-07-24 | 2020-11-06 | 陕西煤业化工技术研究院有限责任公司 | Lithium titanate silicon-based composite negative electrode material and preparation method thereof |
CN112166524A (en) * | 2018-05-29 | 2021-01-01 | 松下知识产权经营株式会社 | Method and system for charging non-aqueous electrolyte secondary battery |
CN112701356A (en) * | 2020-12-14 | 2021-04-23 | 河南环宇惠能能源有限公司 | Formation method of flexible package lithium ion battery |
US20210184276A1 (en) * | 2019-12-11 | 2021-06-17 | Toyota Jidosha Kabushiki Kaisha | Method of producing lithium-ion battery |
WO2021120927A1 (en) * | 2019-12-16 | 2021-06-24 | 比亚迪股份有限公司 | Lithium compensation material and preparation method therefor, and negative electrode and lithium-ion battery |
KR20220059383A (en) * | 2020-11-02 | 2022-05-10 | 에스케이온 주식회사 | Method for quick charge of secondary battery |
CN115084688A (en) * | 2022-06-07 | 2022-09-20 | 北京新能源汽车股份有限公司 | Formation method and application of lithium ion battery |
US20220320608A1 (en) * | 2021-04-01 | 2022-10-06 | Iowa State University Research Foundation, Inc. | Magnetic field-assisted fast charging of lithium-ion batteries |
KR20230045180A (en) * | 2021-09-28 | 2023-04-04 | 주식회사 엘지에너지솔루션 | Secondary battery activation process |
CN118016857A (en) * | 2023-10-26 | 2024-05-10 | 中创新航科技集团股份有限公司 | A negative electrode active material and a lithium ion battery using the same |
-
2023
- 2023-07-27 CN CN202310932384.XA patent/CN117199576B/en active Active
Patent Citations (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000203818A (en) * | 1999-01-13 | 2000-07-25 | Hitachi Chem Co Ltd | Composite carbon particle, its production, negative pole material, negative pole for lithium secondary battery or cell and lithium secondary battery or cell |
KR101511694B1 (en) * | 2013-11-29 | 2015-04-24 | 한화케미칼 주식회사 | Anode active material of lithium rechargeable battery and process for preparing the same |
US20170194672A1 (en) * | 2015-12-30 | 2017-07-06 | Nissan North America, Inc. | High current treatment for lithium ion batteries having metal based anodes |
EP3297070A1 (en) * | 2016-09-19 | 2018-03-21 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Lithium battery comprising a negative electrode with improved service life |
CN106450246A (en) * | 2016-12-28 | 2017-02-22 | 江西正拓新能源科技股份有限公司 | Porous silicon-carbon composite material for lithium ion battery and preparation method of material |
DE102018109698A1 (en) * | 2017-04-25 | 2018-10-25 | GM Global Technology Operations LLC | Method and apparatus for evaluating battery cells containing materials that have a voltage hysteresis |
CN108808140A (en) * | 2018-04-26 | 2018-11-13 | 江西优特汽车技术有限公司 | A kind of power battery charging management method |
CN112166524A (en) * | 2018-05-29 | 2021-01-01 | 松下知识产权经营株式会社 | Method and system for charging non-aqueous electrolyte secondary battery |
US20210184276A1 (en) * | 2019-12-11 | 2021-06-17 | Toyota Jidosha Kabushiki Kaisha | Method of producing lithium-ion battery |
WO2021120927A1 (en) * | 2019-12-16 | 2021-06-24 | 比亚迪股份有限公司 | Lithium compensation material and preparation method therefor, and negative electrode and lithium-ion battery |
CN111900352A (en) * | 2020-07-24 | 2020-11-06 | 陕西煤业化工技术研究院有限责任公司 | Lithium titanate silicon-based composite negative electrode material and preparation method thereof |
KR20220059383A (en) * | 2020-11-02 | 2022-05-10 | 에스케이온 주식회사 | Method for quick charge of secondary battery |
CN112701356A (en) * | 2020-12-14 | 2021-04-23 | 河南环宇惠能能源有限公司 | Formation method of flexible package lithium ion battery |
US20220320608A1 (en) * | 2021-04-01 | 2022-10-06 | Iowa State University Research Foundation, Inc. | Magnetic field-assisted fast charging of lithium-ion batteries |
KR20230045180A (en) * | 2021-09-28 | 2023-04-04 | 주식회사 엘지에너지솔루션 | Secondary battery activation process |
CN115084688A (en) * | 2022-06-07 | 2022-09-20 | 北京新能源汽车股份有限公司 | Formation method and application of lithium ion battery |
CN118016857A (en) * | 2023-10-26 | 2024-05-10 | 中创新航科技集团股份有限公司 | A negative electrode active material and a lithium ion battery using the same |
Non-Patent Citations (3)
Title |
---|
JI D Y: "Research on adaptability of charging strategy for electric vehicle power battery", JOURNAL OF POWER SOURCES, 31 December 2019 (2019-12-31), pages 437 * |
夏向阳: "基于动力锂离子电池健康状态的全寿命周期优化充电策略", 电力科学与技术学报, 31 December 2022 (2022-12-31), pages 17 - 24 * |
金磊: "用于锂电池管理系统的 SOC 估算算法研究", 信息技术与信息化, 31 August 2023 (2023-08-31), pages 20 - 23 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN118315701A (en) * | 2024-05-08 | 2024-07-09 | 江苏正力新能电池技术有限公司 | How to charge the battery |
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